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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Displaying entries 13176 - 13200 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0060903 thrombosis HGNC:3616 Homo sapiens (human) 2212 FCGR2A mutant phenotype evidence used in manual assertion
  • PMID:18983497
  • PMID:20585032
DOID:8584 Burkitt lymphoma HGNC:1699 Homo sapiens (human) 974 CD79B mutant phenotype evidence used in manual assertion
  • PMID:17374736
DOID:10763 hypertension HGNC:3176 Homo sapiens (human) 1906 EDN1 mutant phenotype evidence used in manual assertion
  • PMID:11078355
DOID:3908 lung non-small cell carcinoma HGNC:12766 Homo sapiens (human) 7468 NSD2 mutant phenotype evidence used in manual assertion
  • PMID:34551195
DOID:0060074 ductal carcinoma in situ HGNC:7884 Homo sapiens (human) 4855 NOTCH4 mutant phenotype evidence used in manual assertion
  • PMID:17440163
DOID:1588 thrombocytopenia HGNC:3616 Homo sapiens (human) 2212 FCGR2A mutant phenotype evidence used in manual assertion
  • PMID:10201963
DOID:11446 sciatic neuropathy RGD:620401 Rattus norvegicus (Norway rat) 81509 Bdkrb1 mutant phenotype evidence used in manual assertion
  • PMID:18182225
DOID:10762 portal hypertension RGD:2184 Rattus norvegicus (Norway rat) 24221 Avp mutant phenotype evidence used in manual assertion
  • PMID:18987488
DOID:162 cancer WB:WBGene00001609 Caenorhabditis elegans 176286 glp-1 mutant phenotype evidence used in manual assertion
  • PMID:26120834
  • PMID:33221682
DOID:1824 status epilepticus RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:20643531
DOID:1485 cystic fibrosis SGD:S000001692 Saccharomyces cerevisiae S288C 853671 STE6 mutant phenotype evidence used in manual assertion
  • PMID:7517933
DOID:0050852 limb ischemia HGNC:7876 Homo sapiens (human) 4846 NOS3 mutant phenotype evidence used in manual assertion
  • PMID:12171788
DOID:326 ischemia RGD:2082 Rattus norvegicus (Norway rat) 25233 Akt2 mutant phenotype evidence used in manual assertion
  • PMID:19084003
DOID:2526 prostate adenocarcinoma HGNC:5960 Homo sapiens (human) 3551 IKBKB mutant phenotype evidence used in manual assertion
  • PMID:27196761
DOID:10763 hypertension RGD:3098 Rattus norvegicus (Norway rat) 24590 Mme mutant phenotype evidence used in manual assertion
  • PMID:12011651
DOID:6432 pulmonary hypertension RGD:3812 Rattus norvegicus (Norway rat) 25007 Tacr2 mutant phenotype evidence used in manual assertion
  • PMID:12662901
DOID:2913 acute pancreatitis RGD:620458 Rattus norvegicus (Norway rat) 89808 Cx3cl1 mutant phenotype evidence used in manual assertion
  • PMID:22213034
DOID:3908 lung non-small cell carcinoma HGNC:2976 Homo sapiens (human) 1786 DNMT1 mutant phenotype evidence used in manual assertion
  • PMID:32211850
DOID:0050458 juvenile myelomonocytic leukemia HGNC:2434 Homo sapiens (human) 1437 CSF2 mutant phenotype evidence used in manual assertion
  • PMID:9389708
DOID:707 B-cell lymphoma HGNC:1103 Homo sapiens (human) 6046 BRD2 mutant phenotype evidence used in manual assertion
  • PMID:14563639
DOID:14330 Parkinson's disease WB:WBGene00000898 Caenorhabditis elegans 175410 daf-2 mutant phenotype evidence used in manual assertion
  • PMID:24882066
DOID:6364 migraine RGD:71034 Rattus norvegicus (Norway rat) 65032 Htr7 mutant phenotype evidence used in manual assertion
  • PMID:20236348
DOID:9256 colorectal cancer HGNC:18505 Homo sapiens (human) 54894 RNF43 mutant phenotype evidence used in manual assertion
  • PMID:22202234
  • PMID:22977472
  • PMID:23267878
  • PMID:29473265
DOID:6000 congestive heart failure RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1 mutant phenotype evidence used in manual assertion
  • PMID:24204700
DOID:10652 Alzheimer's disease RGD:2869 Rattus norvegicus (Norway rat) 25718 Igf1r mutant phenotype evidence used in manual assertion
  • PMID:16274856
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025